Issue 29, 2006
From the journal:

Chemical Communications

A modular approach to the synthesis of 2,3,4-trisubstituted tetrahydrofurans†

Christopher G. Nasveschuk,a   Nathan T. Juia  and  Tomislav Rovisa  

a Department of Chemistry, Colorado State University, Fort Collins, CO, USA
E-mail: rovis@lamar.colostate.edu
Fax: +1 970-491-1801
Tel: +1 970-491-7208

Abstract

A highly diastereoselective Lewis acid-mediated [1,3] rearrangement of 1,3-dioxepins is the key step along a modular route to 2,3,4-trisubstituted tetrahydrofurans.

Graphical abstract: A modular approach to the synthesis of 2,3,4-trisubstituted tetrahydrofurans

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DOI
https://doi.org/10.1039/B605438B
Article type
Communication
Submitted
18 Apr 2006
Accepted
08 May 2006
First published
14 Jun 2006

Chem. Commun., 2006, 3119-3121

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A modular approach to the synthesis of 2,3,4-trisubstituted tetrahydrofurans

C. G. Nasveschuk, N. T. Jui and T. Rovis, Chem. Commun., 2006, 3119 DOI: 10.1039/B605438B

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